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Preventing Allograft Rejection by Targeting Immune Metabolism
Chen-Fang Lee, Ying-Chun Lo, Chih-Hsien Cheng, Georg J. Furtmüller, Byoungchol Oh, Vinicius Andrade-Oliveira, Ajit G. Thomas, Caitlyn E. Bowman, Barbara S. Slusher, Michael J. Wolfgang, Gerald Brandacher, Jonathan D. Powell Cell Reports Volume 13, Issue 4, Pages (October 2015) DOI: /j.celrep Copyright © 2015 The Authors Terms and Conditions
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Cell Reports 2015 13, 760-770DOI: (10.1016/j.celrep.2015.09.036)
Copyright © 2015 The Authors Terms and Conditions
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Figure 1 2-DG Combined with Metformin Inhibits T Cell Responses through Suppression of Glycolysis (A and B) The ECAR and OCR of resting CD4+ cells measured in real time under basal conditions and in response to anti-CD3/CD28/cross-linking IgG1 (anti-CD3, 2 μg/ml; anti-CD28, 2 μg/ml; cross-linking IgG1, 1 μg/ml) with or without the presence of individual or combination of drugs (2-DG, 10 mM; metformin, 50 mM). Bar graphs display data of ECAR and OCR measured at the endpoint of the experiment (205 min). Data are shown as mean ± SEM of five measurements. (C and D) Naive splenocytes labeled with cell proliferation dye eFluor 670 were stimulated with anti-CD3 in in the presence of media control, 2-DG alone, metformin alone, or 2-DG + metformin (2-DG, 0.6 mM; metformin, 1 mM). (C) 24-hr IFN-γ secretion to supernatants was interrogated by ELISA. Data are shown as mean ± SEM of three independent samples. (D) 72-hr eFluor dilution of CD4+ and CD8+ T cells. n.s., not significant, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗∗p < (Student’s t test). Data are representative of at least two independent experiments. Cell Reports , DOI: ( /j.celrep ) Copyright © 2015 The Authors Terms and Conditions
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Figure 2 Combined Inhibition of Glycolysis and Glutaminolysis Profoundly Suppresses T Cell Responses (A) Glutaminase activity of CD4+ T cells cultured for 24 hr in different conditions (anti-CD3, 2 μg/ml; anti-CD28, 2 μg/ml; DON, 5 μM; 2-DG, 0.6 mM; metformin, 1 mM). Data are shown as mean ± SEM of three independent experiments. (B and C) Naive WT C57BL/6 splenocytes labeled with eFluor 670 and stimulated with anti-CD3 in medium containing indicated metabolic inhibitors (DON, 5 μM; 2-DG, 0.6 mM; metformin, 1 mM). (B) 24-hr IFN-γ secretion to supernatants as interrogated by ELISA. Data are shown as mean ± SEM of three independent samples. (C) Proliferation of CD4+ and CD8+ T cells at 72 hr measured by dilution of eFluor 670. n.s., not significant, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < (Student’s t test). Data are representative of at least two independent experiments. (D) 3H-acetate incorporation into lipids in preactivated and stimulated CD4+ T cells (anti-CD3, 1 μg/ml; anti-CD28, 2 μg/ml; cross-linking, 0.75 μg/ml) with the presence of 2DG, metformin, DON, or in combination (2DG, 5 mM; metformin, 30 mM; DON, 60 μM). Data are shown as mean ± SEM of three independent samples. ∗∗∗p < (ANOVA). Data are representative of two independent experiments. (E) The phosphorylation state of the S6 ribosomal protein was measured in CD4+ T cells after 30-min stimulation (anti-CD3, 1 μg/ml; anti-CD28, 2 μg/ml; cross-linking 0.75 μg/ml) with the presence of rapamycin, PP242, and metabolic inhibitors (rapamycin, 1 μM; pp242, 1 μM; 2DG, 5 mM, metformin, 30 mM; DON, 60 μM). Data are representative of two independent experiments. Cell Reports , DOI: ( /j.celrep ) Copyright © 2015 The Authors Terms and Conditions
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Figure 3 Metabolic Inhibitors Suppress the Proliferation and Function of Antigen-Specific T Cells while Increasing the Relative Frequency of Tregs In Vivo (A–D) OT-II (Thy1.1+) CD4+ T cells were adoptively transferred into WT (Thy1.2+) recipient mice. The recipients were infected with OVA-expressing vaccinia virus and treated with vehicle, 2-DG + metformin, or 2-DG + metformin + DON (2-DG, 500 mg/kg once daily; metformin, 150 mg/kg once daily; DON, 1.6 mg/kg once every other day) for 3 days. Splenocytes from the recipients were harvested at day 4 to interrogate the frequency of antigen-specific T cells and regulatory T cells. (A) Percentage of Thy1.1+ cells relative to CD4+ cells were analyzed by flow cytometry (left) and plotted as cumulative data (right). (B) OT-II cells were rechallenged with OVA peptide class II (10 μg/ml) ex vivo for 24 hr. The supernatants were interrogated for IFN-γ production by ELISA. Data are mean ± SEM (n = 6). (C) Percentage of Foxp3+ cells relative to CD4+ cells (left) and plotted as cumulative data (right). (D) The ratio of OVA-specific Foxp3+ T cells to effector cells. (E–G) OT-I (Thy1.1+) CD8+ T cells were adoptively transferred into WT (Thy1.2+) recipient mice. The hosts were infected with vaccinia-OVA and treated with vehicle, 2-DG + metformin, or triple therapy for 5 days. Host splenocytes were harvested at day 6 to interrogate the proliferation and function of antigen-specific CD8+ T cells. (E) The percentage Thy1.1+ cells relative to CD8+ cells was analyzed by flow cytometry (left) and plotted as cumulative data (right). (F) The percentage IFN-γ-producing cells relative to CD8+ cells (left) and plotted as cumulative data (right). (G) OT-I cells were rechallenged with OVA peptide class I (10 μg/ml) ex vivo for 24 hr. The supernatants were interrogated for IFN-γ production by ELISA. Data are mean ± SEM (n = 5–6). (H) The ability of metabolic inhibitors to suppress endogenous effector CD8+ T cell development was assessed with an in vivo CTL assay. Percent of specific killing was determined at 10 hr after transferring target cells. Data are mean ± SEM (n = 3 mice/group). Each symbol represents an individual mouse. Horizontal lines indicate mean ± SEM. n.s., not significant, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < (Student’s t test). Data are representative of more than three independent experiments. Cell Reports , DOI: ( /j.celrep ) Copyright © 2015 The Authors Terms and Conditions
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Figure 4 Metabolic Inhibitors Promote Allograft Survival
(A) BALB/c to C57BL/6 skin graft survival, as monitored daily by assessment of macroscopic signs of rejection. (B) Representative photomicrographs of skin graft histology (H&E staining) on post-transplant days 7 and 40 under an optical microscope (outlet, ×100; inlet: ×200). (C) BALB/c to C57BL/6 heart graft survival, as monitored daily by palpation of heart beating. (D) Representative photomicrographs of cardiac graft histology (H&E staining) on indicated post-transplant day under an optical microscope (outlet, ×200; inlet, ×400). The anti-metabolic treatment was started from the day of graft (day 0) until rejection in both models. The dosages of all drugs were the same as described in Figure 3. ∗∗p < 0.01, ∗∗∗∗p < (log-rank analysis). Data are representative of two independent experiments. Cell Reports , DOI: ( /j.celrep ) Copyright © 2015 The Authors Terms and Conditions
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